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A biotechnologist wanted to create a col...

A biotechnologist wanted to create a colony of E.coli possessing the plasmid pBR322, sensitive to Tetracycline. Which one of the following restriction sites would he use to ligate a foreign DNA ?

A

Sal I

B

Pvu I

C

Eco RI

D

Hind III

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To solve the question regarding the creation of a colony of E. coli possessing the plasmid pBR322 that is sensitive to Tetracycline, we can follow these steps: ### Step-by-Step Solution: 1. **Understand the Objective**: The biotechnologist wants to create a colony of E. coli that is sensitive to Tetracycline. This means that the E. coli must lose its resistance to Tetracycline. 2. **Identify the Plasmid**: The plasmid in question is pBR322. This plasmid contains genes that confer resistance to antibiotics, including Tetracycline. 3. **Locate the Restriction Sites**: The pBR322 plasmid has specific restriction sites where foreign DNA can be inserted. The relevant sites include: - BamHI - SalI - EcoRI - HindIII - PvuI 4. **Determine the Impact of Insertion**: To make the E. coli sensitive to Tetracycline, the foreign DNA must be inserted into the Tetracycline resistance gene. This will disrupt the gene, leading to the loss of resistance. 5. **Identify the Correct Restriction Site**: - The BamHI and SalI sites are located within the Tetracycline resistance gene. - Inserting foreign DNA at either of these sites will disrupt the gene and make the E. coli sensitive to Tetracycline. - The question asks for one restriction site, and since SalI is mentioned, we will choose that. 6. **Conclusion**: The biotechnologist should use the SalI restriction site to ligate the foreign DNA, as it will effectively disrupt the Tetracycline resistance gene in pBR322. ### Final Answer: The restriction site that should be used to ligate the foreign DNA is **SalI**. ---

To solve the question regarding the creation of a colony of E. coli possessing the plasmid pBR322 that is sensitive to Tetracycline, we can follow these steps: ### Step-by-Step Solution: 1. **Understand the Objective**: The biotechnologist wants to create a colony of E. coli that is sensitive to Tetracycline. This means that the E. coli must lose its resistance to Tetracycline. 2. **Identify the Plasmid**: The plasmid in question is pBR322. This plasmid contains genes that confer resistance to antibiotics, including Tetracycline. ...
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Which one of the following restriction enzyme can cut "Tet"^R site of pBR322 ?

Which one of the following is commonly used in transfer of foreign DNA into crop plants?

Knowledge Check

  • Which one of the following is commonly used in transfer of foreign DNA into crop plants?

    A
    Trichoderma harzianum
    B
    Meloidogyne incognita
    C
    Agrobacterium tumefaciens
    D
    Penicillium expansum
  • In pBR322, tetracycline resistance gene (tet^(R)) has recognition site for which of the following restriction endonuclease ? 1) Hindlll 2) BamHl 3) EcoRl 4) Pstl

    A
    1) Hindlll
    B
    2) BamHl
    C
    3) EcoRl
    D
    4) Pstl
  • Similar Questions

    Explore conceptually related problems

    Which of the following restriction endonucleases cannot be used while using pBR322 as a cloning vector ?

    In order to insert alien DNA at the site of tetracycline resistance gene in pBR322 the restriction endonuclease used can be :

    If you can ligate foreign DNA at the BamHI site in the vector pBR322, which of the following will occur?

    Which of the following restriction enzyme site is present in nucleotide sequence of ampicillin resistance gene in pBR322?

    I. Transform bacteria with recombinant DNA molecule. II. Cut the plasmid DNA using restriction enzymes. III. Extract plasmid DNA from bacteria cells. IV. Hydrogen-bond the plasmid DNA to non-plasmid DNA fragments. V. Use ligate to seal plasmid DNA to non-plasmid DNA. From the given list, which of the following is the most logical sequence of steps for splicing foregain DNA into a plasmid and inserting the plasmid into a bacterium ?

    If we ligate a foreign, DNA at the Barn HI site of tetracycline resistance gene in pBR322 the recombinant plasmid will: